Summary: Coordinates and manages the department/center's research portfolio. Maintains working ... Provides monitoring, review and tracking of clinical data and preparation of study specific ...
Summary: Coordinates and manages the department/center's research portfolio. Maintains working ... Provides monitoring, review and tracking of clinical data and preparation of study specific ...
Clinical Research Associate I
$25 - $27/hr
... coordination across internal teams and external partners. The position supports translational ... At least 2 years of hands-on clinical sample management or clinical research operations experience ...
New
Clinical Research Associate I
$25 - $27/hr
... coordination across internal teams and external partners. The position supports translational ... At least 2 years of hands-on clinical sample management or clinical research operations experience ...
New
Clinical Research Associate I
Columbus, OH · On-site
$25 - $27/hr
This Research Associate I role in Translational Biology focuses on clinical research support in a ... coordination across internal teams and external partners. The position supports translational ...
New
Clinical Research Associate I
Columbus, OH · On-site
$25 - $27/hr
This Research Associate I role in Translational Biology focuses on clinical research support in a ... coordination across internal teams and external partners. The position supports translational ...
New
Research Regulatory Coordinator - RI Pulmonary Med
Columbus, OH · On-site
$23.50 - $31.25/hr
Creates the initial study administrative binder required for the clinical research project. Maintains study binders, files documents timely, and reviews binders prior to monitor visits to ensure ...
Research Regulatory Coordinator - RI Pulmonary Med
Columbus, OH · On-site
$23.50 - $31.25/hr
Creates the initial study administrative binder required for the clinical research project. Maintains study binders, files documents timely, and reviews binders prior to monitor visits to ensure ...
Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; * Verify adequate investigator qualifications, training and resources, including ...
Communication with the medical site staff including coordinators, clinical research physicians, and their site staff; * Verify adequate investigator qualifications, training and resources, including ...
... coordination of studies; participates in recruitment of study participants; performs behavioral or diagnostic testing; assists with collection maintenance & reporting of clinical research data.
... coordination of studies; participates in recruitment of study participants; performs behavioral or diagnostic testing; assists with collection maintenance & reporting of clinical research data.
Pharmacist-PRN
Columbus, OH · On-site
$56.25 - $67.50/hr
Trains Research Pharmacy Technician, clinical research coordinators or any other appropriately ... Ability to perform overnight business travel * Basic computer skills to include Word, Excel, as ...
Quick apply
Pharmacist-PRN
Columbus, OH · On-site
$56.25 - $67.50/hr
Trains Research Pharmacy Technician, clinical research coordinators or any other appropriately ... Ability to perform overnight business travel * Basic computer skills to include Word, Excel, as ...
Pharmacist-PRN
$54.50 - $65.50/hr
Trains Research Pharmacy Technician, clinical research coordinators or any other appropriately ... Ability to perform overnight business travel * Basic computer skills to include Word, Excel, as ...
Pharmacist-PRN
$54.50 - $65.50/hr
Trains Research Pharmacy Technician, clinical research coordinators or any other appropriately ... Ability to perform overnight business travel * Basic computer skills to include Word, Excel, as ...
Pharmacist-PRN
Columbus, OH · On-site
$54.50 - $65.50/hr
Trains Research Pharmacy Technician, clinical research coordinators or any other appropriately ... Ability to perform overnight business travel * Basic computer skills to include Word, Excel, as ...
Pharmacist-PRN
Columbus, OH · On-site
$54.50 - $65.50/hr
Trains Research Pharmacy Technician, clinical research coordinators or any other appropriately ... Ability to perform overnight business travel * Basic computer skills to include Word, Excel, as ...
Creates the initial study administrative binder required for the clinical research project. Maintains study binders, files documents timely, and reviews binders prior to monitor visits to ensure ...
Creates the initial study administrative binder required for the clinical research project. Maintains study binders, files documents timely, and reviews binders prior to monitor visits to ensure ...
Nurse Practitioner (NP) or Physician Assistant (PA)-PRN
Columbus, OH · On-site
$105.30K - $136.20K/yr
This role will require working closely with the Clinical Research Coordinators, assisting in tasks that relate to the conduct of clinical trials. This position is essential to providing support to ...
Quick apply
Nurse Practitioner (NP) or Physician Assistant (PA)-PRN
Columbus, OH · On-site
$105.30K - $136.20K/yr
This role will require working closely with the Clinical Research Coordinators, assisting in tasks that relate to the conduct of clinical trials. This position is essential to providing support to ...
... on clinical sample management, sample logistics, and coordination across internal teams and ... Provide research and operational support for translational biology efforts across cell and gene ...
Quick apply
... on clinical sample management, sample logistics, and coordination across internal teams and ... Provide research and operational support for translational biology efforts across cell and gene ...
... on clinical sample management, sample logistics, and coordination across internal teams and ... Provide research and operational support for translational biology efforts across cell and gene ...
Quick apply
... on clinical sample management, sample logistics, and coordination across internal teams and ... Provide research and operational support for translational biology efforts across cell and gene ...
Research Associate I
Westerville, OH · On-site
Research Associate I - Translational Biology INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO ... on clinical sample management, sample logistics, and coordination across internal teams and ...
Quick apply
Research Associate I
Westerville, OH · On-site
Research Associate I - Translational Biology INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO ... on clinical sample management, sample logistics, and coordination across internal teams and ...
Lab Supervisor
Columbus, OH · On-site
... clinical research safety laboratory. • Assist Lab Manager with the directing and coordinating laboratory personnel to ensure quality, accuracy, and timeliness of laboratory testing and reporting ...
Quick apply
Lab Supervisor
Columbus, OH · On-site
... clinical research safety laboratory. • Assist Lab Manager with the directing and coordinating laboratory personnel to ensure quality, accuracy, and timeliness of laboratory testing and reporting ...
Program Coordinator
Columbus, OH · On-site
Coordinates subcontracts with other sites and the Sponsored Projects Office, develops and ... Two years clinical research experience or project management experience. Physical Requirements:
Program Coordinator
Columbus, OH · On-site
Coordinates subcontracts with other sites and the Sponsored Projects Office, develops and ... Two years clinical research experience or project management experience. Physical Requirements:
Data Entry Clerk
Columbus, OH · On-site
$16.50 - $22/hr
Data Entry Coordinator/Clerk Location: About Company: Who is ERG? ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development ...
Quick apply
Data Entry Clerk
Columbus, OH · On-site
$16.50 - $22/hr
Data Entry Coordinator/Clerk Location: About Company: Who is ERG? ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development ...
... research protocols, university staff, affiliates, and patients; * Work with CTO Managers and coordinators as needed to ensure understanding of study protocols; * Reviews, evaluates, and compiles ...
... research protocols, university staff, affiliates, and patients; * Work with CTO Managers and coordinators as needed to ensure understanding of study protocols; * Reviews, evaluates, and compiles ...
This role ensures efficient coordination of study related activities by managing communication ... Thorough understanding or ability to learn concepts and terminology related to clinical research ...
This role ensures efficient coordination of study related activities by managing communication ... Thorough understanding or ability to learn concepts and terminology related to clinical research ...
We conduct research and development, manage national laboratories, design and manufacture products ... coordination of project resources, schedules, deliverables, and cross-project dependencies
We conduct research and development, manage national laboratories, design and manufacture products ... coordination of project resources, schedules, deliverables, and cross-project dependencies
Overnight Clinical Research Coordinator information
See Columbus, OH salary details
$15.09 - $17.41
2% of jobs
$17.41 - $19.74
7% of jobs
$19.74 - $22.06
12% of jobs
$22.51 is the 25th percentile. Wages below this are outliers.
$22.06 - $24.38
19% of jobs
The median wage is $25.54 / hr.
$24.38 - $26.70
19% of jobs
$26.70 - $29.02
15% of jobs
$29.14 is the 75th percentile. Wages above this are outliers.
$29.02 - $31.35
11% of jobs
$31.35 - $33.67
5% of jobs
$33.67 - $35.99
4% of jobs
$35.99 - $38.31
3% of jobs
$38.31 - $40.63
2% of jobs
$15
$27
$40
How much do overnight clinical research coordinator jobs pay per hour?
As of May 28, 2026, the average hourly pay for overnight clinical research coordinator in Columbus, OH is $27.71, according to ZipRecruiter salary data. Most workers in this role earn between $22.50 and $29.95 per hour, depending on experience, location, and employer.
What is the difference between Overnight Clinical Research Coordinator vs Clinical Research Coordinator?
| Aspect | Overnight Clinical Research Coordinator | Clinical Research Coordinator |
|---|---|---|
| Work Hours | Primarily overnight shifts | Daytime hours, flexible depending on study |
| Certifications | Often requires CPR, research certifications | Similar certifications, may vary by employer |
| Work Environment | Hospitals, clinics, research sites during night shifts | Research centers, hospitals, clinics during day shifts |
| Job Responsibilities | Monitoring overnight patient visits, data collection, ensuring protocol adherence during night hours | Participant recruitment, data management, study coordination during regular hours |
In summary, the main difference lies in work hours and shift timing. Overnight Clinical Research Coordinators focus on night shifts, handling overnight patient visits and data collection, while Clinical Research Coordinators typically work during daytime hours managing various study tasks.
What are popular job titles related to Overnight Clinical Research Coordinator jobs in Columbus, OH? For Overnight Clinical Research Coordinator jobs in Columbus, OH, the most frequently searched job titles are:
What job categories do people searching Overnight Clinical Research Coordinator jobs in Columbus, OH look for? The top searched job categories for Overnight Clinical Research Coordinator jobs in Columbus, OH are:
What cities near Columbus, OH are hiring for Overnight Clinical Research Coordinator jobs? Cities near Columbus, OH with the most Overnight Clinical Research Coordinator job openings:
Fetal Center - Clinical Research Program Coordinator
Nationwide Children's HospitalColumbus, OH • On-site
Full-time
Posted yesterday
Nationwide Children's Hospital rating
7.1
Based on 126 frontline employees who took The Breakroom Quiz
431st of 989 rated hospitals
Job description
Overview:
Job Description Summary:
Coordinates and manages the department/center's research portfolio. Maintains working knowledge of projects in process as well as funded projects including grant budgets and IRB protocols. Coordinates subcontracts with other sites and the Sponsored Projects Office, develops and implements processes across multiple study sites, and maintains documents to ensure effective, efficient and compliant project progress.
Job Description:
Essential Functions:
Education Requirement:
Bachelor's degree preferred or Associate degree with two years clinical research experience or project management experience.
Certifications:
ACRP or SOCRA certification, preferred.
Skills:
Experience:
Two years clinical research experience or project management experience.
Physical Requirements:
OCCASIONALLY: Bend/twist, Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Lifting / Carrying: 21-40 lbs, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Pushing / Pulling: 41-60 lbs, Reaching above shoulder, Squat/kneel
FREQUENTLY: Sitting, Standing, Walking
CONTINUOUSLY: Audible speech, Computer skills, Decision Making, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Peripheral vision, Problem solving, Repetitive hand/arm use, Seeing - Far/near
Additional Physical Requirements performed but not listed above:
(not specified)
"The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individuals so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under their supervision. EOE M/F/Disability/Vet"
Job Description Summary:
Coordinates and manages the department/center's research portfolio. Maintains working knowledge of projects in process as well as funded projects including grant budgets and IRB protocols. Coordinates subcontracts with other sites and the Sponsored Projects Office, develops and implements processes across multiple study sites, and maintains documents to ensure effective, efficient and compliant project progress.
Job Description:
Essential Functions:
- Responsible for administrative management, organization of, and participation in program meetings and teleconferences, including scientific meetings with corporate and non-profit partners, teaching conferences, grand rounds, journal club, research seminars, and CME programs.
- Works with Sponsored Projects Officer to manage program and project funds and dissemination of funding to collaborations sites in addition to the subcontracts with other sites.
- Provides funding opportunity notifications to PI's.
- Collaborates with department/center investigators in the development of IRB protocols, grant submissions and scientific publications.
- Coordinates personnel needs for the program and projects; oversees and organizes training.
- Track projects and initiatives to ensure they move forward based on both timelines and budget; report to PI when progress is lacking and identifies needed action.
- May be responsible for administrative management of multiple protocols; plays a central role in the communication between NCH/RI and site; will act as liaison with other departments necessary to complete program projects (i.e., Data Management, Biostats, Medical Writing, Regulatory Compliance, etc.).
- Manages and oversees IRB process for program projects and associated sites, ensuring sites are submitting accurate and timely IRB submissions, and maintain associated regulatory documents.
- Helps facilitate creation of source documents that ensure systematic data collection and/or aid in protocol execution and management and record keeping.
- Collects and controls research data and subject information from sites as needed/requested; tracks screening and enrollment data across multiple sites/multiple projects.
- Provides monitoring, review and tracking of clinical data and preparation of study specific documents according to FDA regulations QA process implementation, maintenance and documentation; data entry; and maintenance of regulatory documents for multiple sites; multiple protocols.
- Work with principal investigators at each site to establish multi-site monitoring plans for investigator-initiated projects.
Education Requirement:
Bachelor's degree preferred or Associate degree with two years clinical research experience or project management experience.
Certifications:
ACRP or SOCRA certification, preferred.
Skills:
- Demonstrated leadership skills
- Strong organizational skills
- Exceptional interpersonal, written and verbal communication
- Ability to filter information, discern importance and initiate plan for project completion
- Self-directed, results driven with the ability to manage workload.
- Ability to work independently and as part of a team.
- Working knowledge of data management software.
Experience:
Two years clinical research experience or project management experience.
Physical Requirements:
OCCASIONALLY: Bend/twist, Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Lifting / Carrying: 21-40 lbs, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Pushing / Pulling: 41-60 lbs, Reaching above shoulder, Squat/kneel
FREQUENTLY: Sitting, Standing, Walking
CONTINUOUSLY: Audible speech, Computer skills, Decision Making, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Peripheral vision, Problem solving, Repetitive hand/arm use, Seeing - Far/near
Additional Physical Requirements performed but not listed above:
(not specified)
"The above list of duties is intended to describe the general nature and level of work performed by individuals assigned to this classification. It is not to be construed as an exhaustive list of duties performed by the individuals so classified, nor is it intended to limit or modify the right of any supervisor to assign, direct, and control the work of employees under their supervision. EOE M/F/Disability/Vet"
What Nationwide Children's Hospital employees say
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About Nationwide Children's Hospital
Sourced by ZipRecruiter
Nationwide Children's Hospital, established in 1894, is a leading pediatric healthcare system based in Columbus, Ohio, United States. They serve as a primary pediatric network, providing wellness, preventive, diagnostic, treatment, and rehabilitative care for infants, children, adolescents, and adults with congenital disease. Being the third-largest pediatric hospital in the nation, Nationwide Children's Hospital prides itself on its relentless commitment to children and their families, driven by their core values of respect, integrity, determination, empathy, and solidarity. The institution's comprehensive mission is to enhance the health of children by providing high-quality, family-centered care, conducting groundbreaking research, advocating for pediatric health, and training top healthcare professionals.
Industry
Hospitals
Company size
10,000+ Employees
Headquarters location
Columbus, OH, US
Year founded
1892